inforMED
InjuryMBP

NA

Received Nov 5, 2014

Report 1030489-2014-04226 · MDR key 4228174

Device

Generic name

Filler, Bone Void, Osteoinduction (w/o Human Growth Factor)

Model number

NA

Catalog number

006010

Lot number

4094040027

Product problems

  • Adverse Event Without Identified Device or Use Problem

Patient

Not reported

  • Unspecified Infection

Narrative

Additional Manufacturer Narrative

(B)(4). NEITHER THE PRODUCT NOR APPLICABLE IMAGING FILMS WERE RETURNED TO THE MANUFACTURER FOR EVALUATION; THEREFORE, THE CAUSE OF THE EVENT CANNOT BE DETERMINED.

Description of Event or Problem

IT WAS REPORTED THAT AFTER AN UNSPECIFIED SPINAL SURGERY THAT THE PATIENT HAD AN INFECTION POST-OPERATIVELY.

Additional Manufacturer Narrative

IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.